Term Name:	nuclear type mitochondrial complex I deficiency 35
Synonyms:	MC1DN35
Definition:	A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFB10 gene on chromosome 16p13.3.
Ontology:	Human Disease [DOID:0112139]   ( DOID:0112139 )